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Impact of Receipt of Hearing Aid on Depressive Symptoms in Older Adults

Impact of Receipt of Hearing Aid on Depressive Symptoms in Older Adults

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300069838
Enrollment
Unknown
Registered
2023-03-27
Start date
2023-04-01
Completion date
Unknown
Last updated
2023-05-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

depression,hearing loss

Interventions

Experimental group:Hearing aids
Control group:NA

Sponsors

Shandong University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: (1) older adults aged=60 years; (2) presence of depressive symptoms (a score of Geriatric Depression Scale-15 (GDS-15) 0-4 is considered to be within the normal range, =5 indicates presence of depressive symptoms); (3) diagnosed with untreated adult-onset bilateral HL with a pure-tone average (PTA) =30 dB and<70 dB (at frequencies 500,1000,2000 and 4000 Hz); (4) Considered likely to benefit from amplification (i.e. participants have a Word Recognition in Quiet score=60% correct in the better-hearing ear)

Exclusion criteria

Exclusion criteria: (1) Vascular Dementia, probable Alzheimers disease, or Parkinsons Disease diagnosis or Mini-Mental State Examination (MMSE) score of =24; (2) history of major psychiatric illness, mania, bipolar disorder, substance use disorder within the past 12 months, or had current suicidal ideation; (3) severe or unstable disabling comorbid disease (terminal cancer, hepatic encephalopathy, end-stage pulmonary disease requiring home oxygen therapy); (4) history of a hearing aid use within the past 12 months; (5) medical contraindication to use of hearing aids (i.e. visible deformity of the ear, perforated eardrum combined inflammation, fluid or drainage from the ear within the past 90 days); (6) conductive HL with air-bone gap >15dB in two or more contiguous frequencies in both ears that cannot be resolved; (7) history of significant retro-cochlear pathology or organic lesion responsible for HL; (8) reported unwilling to purchase HA or wear HA on daily basis; (9) presence of severe tinnitus, or a diagnosis of Meniere’s disease.

Design outcomes

Primary

MeasureTime frame
depressive symptoms;hearing status;

Secondary

MeasureTime frame
social isolation;lonliness;basical activities of daily living scale, BADLs;

Countries

China

Contacts

Public ContactFan Jiang

shandong university

jiang.fan@sdu.edu.cn+86 18615511566

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026